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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366863Generated: November 2, 2026

2-Chloro-4-(trifluoromethyl)benzenesulfonyl chloride → HCID 57718182, compound

https://huagongshe.com/reaction/1366863

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-(trifluoromethyl)benzenesulfonyl chlorideHCID 2736675—
ReactantHCID 57718211HCID 57718211—
SolventPyridineHCID 1049—
ProductHCID 57718182HCID 5771818210.9%

Reaction Steps

5-Methyl-6-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-pyridazin-3-ylamine (110 mgs), 2-chloro-4-trifluoromethylbenzenesulfonyl chloride (160 mgs) and pyridine (1 ml) were heated at 50° C. under nitrogen for 72 hours. All volatiles were removed and the residue purified by Preparative HPLC to give 2-chloro-N-{5-methyl-6-[4-(piperidine-1-sulfonyl)-phenylsulfanyl]-pyridazin-3-yl}-4-trifluoromethyl-benzenesulfonamide 20 mg. 1H NMR (CDCl3) 8.25 (1H, d) 7.75 (2H, m) 7.7 (1H, s) 7.6 (3H, m) 6.95 (1H, s) 3.0 (4H, m) 2.3 (3H, s) 1.6 (4H, m) 1.45 (2H, m). LCMS Polarity/Scan type: Negative Q1 Scan. M.wt. 605 (—H), 607 (—H). Retention time 7.05 minutes. HPLC:—MS8. Retention time 4.99 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893077B2
Source datasetuspto-grants-2011_02
ORD IDord-ce005d0950dd4c988115e0b6a115d761
Source noteuspto-grants-2011_02